Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders (2024)
- Authors:
- Tolezano, Giovanna Cantini
- Bastos, Giovanna Civitate
- Costa, Silvia Souza da
- Scliar, Marília de Oliveira
- Souza, Carolina Fischinger Moura de
- Linden Jr, Hélio Van Der
- Fernandes, Walter Luiz Magalhães
- Otto, Paulo A
- Vianna-Morgante, Angela M
- Haddad, Luciana Amaral
- Honjo, Rachel Sayuri
- Yamamoto, Guilherme Lopes
- Kim, Chong Ae
- Rosenberg, Carla
- Jorge, Alexander Augusto de Lima
- Bertola, Débora Romeo
- Krepischi, Ana Cristina Victorino
- USP affiliated authors: OTTO, PAULO ALBERTO - IB ; MORGANTE, ANGELA MARIA VIANNA - IB ; HADDAD, LUCIANA AMARAL - IB ; YAMAMOTO, GUILHERME LOPES - Interunidades em Bioinformática ; ROSENBERG, CARLA - IB ; JORGE, ALEXANDER AUGUSTO DE LIMA - FM ; BERTOLA, DÉBORA ROMEO - IB ; KREPISCHI, ANA CRISTINA VICTORINO - IB ; TOLEZANO, GIOVANNA CANTINI - IB ; COSTA, SILVIA SOUZA DA - IB
- Unidades: IB; Interunidades em Bioinformática; FM
- DOI: 10.1007/s12035-023-03894-8
- Subjects: MICROCEFALIA; NEUROLOGIA; GENÉTICA
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Heidelberg
- Date published: 2024
- Source:
- Título: Molecular Neurobiology
- ISSN: 1559-1182
- Volume/Número/Paginação/Ano: on-line, 2024
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
TOLEZANO, Giovanna Cantini et al. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders. Molecular Neurobiology, 2024Tradução . . Disponível em: https://doi.org/10.1007/s12035-023-03894-8. Acesso em: 29 dez. 2025. -
APA
Tolezano, G. C., Bastos, G. C., Costa, S. S. da, Scliar, M. de O., Souza, C. F. M. de, Linden Jr, H. V. D., et al. (2024). Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders. Molecular Neurobiology. doi:10.1007/s12035-023-03894-8 -
NLM
Tolezano GC, Bastos GC, Costa SS da, Scliar M de O, Souza CFM de, Linden Jr HVD, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AA de L, Bertola DR, Krepischi ACV. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders [Internet]. Molecular Neurobiology. 2024 ;[citado 2025 dez. 29 ] Available from: https://doi.org/10.1007/s12035-023-03894-8 -
Vancouver
Tolezano GC, Bastos GC, Costa SS da, Scliar M de O, Souza CFM de, Linden Jr HVD, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AA de L, Bertola DR, Krepischi ACV. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders [Internet]. Molecular Neurobiology. 2024 ;[citado 2025 dez. 29 ] Available from: https://doi.org/10.1007/s12035-023-03894-8 - KIF11 microdeletion is associated with microcephaly, chorioretinopathy and intellectual disability
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Informações sobre o DOI: 10.1007/s12035-023-03894-8 (Fonte: oaDOI API)
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